Terry G J Derks
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Explore the profile of Terry G J Derks including associated specialties, affiliations and a list of published articles.
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99
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1155
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Recent Articles
1.
Haijer-Schreuder A, Jager E, Derks T
Acta Paediatr
. 2025 Mar;
PMID: 40038046
No abstract available.
2.
Veldman A, Sikkema-Raddatz B, Derks T, van Karnebeek C, Kiewiet M, Mulder M, et al.
Int J Neonatal Screen
. 2025 Jan;
11(1.
PMID: 39846587
The biomarker-based Dutch Newborn Screening (NBS) panel (as of 2024) comprises 19 inherited metabolic disorders (IMDs). With the use of next-generation sequencing (NGS) as a first-tier screen, NBS could expand...
3.
Kiyuna L, Krishnamurthy K, Homan E, Langelaar-Makkinje M, Gerding A, Bos T, et al.
Commun Biol
. 2024 Nov;
7(1):1479.
PMID: 39521914
Fasting hypoglycemia is a severe and incompletely understood symptom of various inborn errors of metabolism (IEM). Precision-cut liver slices (PCLS) represent a promising model for studying glucose production ex vivo....
4.
Gross-Valle C, Jacobs T, Dijck-Brouwer J, Lubberts J, Bakker B, Bakker S, et al.
J Inherit Metab Dis
. 2024 Oct;
48(1):e12801.
PMID: 39460557
The urinary metabolite tetraglucoside (Glc4) is a potential biomarker for hepatic glycogen storage diseases (GSDs). Glc4 is believed to reflect body glycogen content and/or turnover. However, dietary polysaccharide intake may...
5.
Rossi A, Ruoppolo M, Fedele R, Pirozzi F, Rosano C, Auricchio R, et al.
J Lipid Res
. 2024 Sep;
65(10):100651.
PMID: 39306041
Glycogen storage disease type Ia (GSDIa) is a rare, inherited glucose-6-phosphatase-α (G6Pase-α) deficiency-induced carbohydrate metabolism disorder. Although hyperlipidemia is a hallmark of GSDI, the extent of lipid metabolism disruption remains...
6.
Overduin R, Venema A, Lubout C, Fokkert-Wilts M, de Boer F, Schreuder A, et al.
Mol Genet Metab
. 2024 Sep;
143(1-2):108573.
PMID: 39243574
Background: Cohort data on continuous glucose monitoring (CGM) metrics are scarce for liver glycogen storage diseases (GSDs) and idiopathic ketotic hypoglycemia (IKH). The aim of this study was to retrospectively...
7.
Overduin R, Grunert S, Besouw M, Bolhuis M, Groen J, Schreuder A, et al.
J Inherit Metab Dis
. 2024 May;
47(5):1018-1027.
PMID: 38802119
Renal proximal tubulopathy in Fanconi-Bickel syndrome is caused by impaired basolateral glucose transport via GLUT2 and consequently, intracellular accumulation of glucose and glycogen. SGLT2 inhibitors act on apical glucose reabsorption...
8.
Grunert S, Gautschi M, Baker J, Boyer M, Burlina A, Casswall T, et al.
Mol Genet Metab
. 2024 May;
142(2):108486.
PMID: 38733639
Empagliflozin has been successfully repurposed for treating neutropenia and neutrophil dysfunction in patients with glycogen storage disease type 1b (GSD 1b), however, data in infants are missing. We report on...
9.
Rossi A, Simeoli C, Pivonello R, Salerno M, Rosano C, Brunetti B, et al.
Rev Endocr Metab Disord
. 2024 Mar;
25(4):707-725.
PMID: 38556561
Hepatic glycogen storage diseases constitute a group of disorders due to defects in the enzymes and transporters involved in glycogen breakdown and synthesis in the liver. Although hypoglycemia and hepatomegaly...
10.
Wolfsdorf J, Derks T, Drachmann D, Shah P, Thornton P, Weinstein D
Horm Res Paediatr
. 2024 Mar;
:1-12.
PMID: 38513624
Sick children often have a decreased appetite and experience vomiting and diarrhea; however, hypoglycemia (plasma glucose concentration ≤50 mg/dL or 2.8 mmol/L) is rare. Ketotic hypoglycemia (KH) is the most...